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Potassium Cyanide → 2-Amino-2-cyano-5-methoxy-1,2,3,4-tetrahydronaphthalene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Cyanide | HCID 9032 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 5-Methoxy-2-tetralone | HCID 259194 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-Amino-2-cyano-5-methoxy-1,2,3,4-tetrahydronaphthalene | HCID 9990431 | — |
反応手順
112 mmol of potassium cyanide and 116 mmol of ammonium chloride ate added successively to a solution, maintained under nitrogen and with stirring, containing 110 mmol of 5-methoxy-3,4-dihydronaphthalen-2(1H)-one in 90 ml of ethanol and 50 ml of water. The whole mixture is stirred for 20 hours at 20° C. and then concentrated under vacuum. The residue is taken up in 200 ml of ethyl acetate. This phase is then washed with water and extracted with 1N hydrochloric acid. The acid phase is basified with 35% sodium hydroxide solution and extracted with methyl acetate. The combined organic phases are dried and evaporated under vacuum and lead to the expected product in the solid form.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05464859 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-ba8afc10f72a433885205de1993275b0 |
| 出典メモ | uspto-grants-1995_11 |